presentation on genome sequencing

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Presentation on genome sequencing

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Presentation on genome sequencing . Genome : the complete set of gene of an organism. Genome annotation: the process by which the genes, control sequences and other interesting features are identified. First DNA completely sequenced: (5386 bp ) bacteriophage ØX174 in 1975. - PowerPoint PPT Presentation

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Page 1: Presentation on genome sequencing

Presentation on genome sequencing

Page 2: Presentation on genome sequencing

Genome: the complete set of gene of an organism

Genome annotation: the process by which the genes, control sequences and other interesting features are identified.

•First DNA completely sequenced: (5386 bp) bacteriophage ØX174 in 1975.• SV40 virus: (5243 bp) in 1977.•pBR322: (4363 bp) in 1978.•The first chromosome sequence: chromosome III of the yeast Saccharomyces cerevisiae, in 1992, and was completed in 1996.

Page 3: Presentation on genome sequencing

Why genome sequencing is required?

GENOME SEQUENCING

GENOMICS POST GENOMICS

BIOINFORMATICS

ANALYSIS e.g. GENE LOCATION, CONTROL SEQUENCES

FUNCTION OF UNKNOWN GENE SEQUENCE DATA CORRECT ASSAMBLY

OF GENE SEQUENCES

COMPUTETRIZED ASSAMBLY, EXAMINATION AND PREDICTION OF GENES

LARGE AMOUNT OF DATA STORAGE

Page 4: Presentation on genome sequencing

TWO BASIC APPROACHES FOR GENOME SEQUENCING

Page 5: Presentation on genome sequencing

BASIC PROCEDURE

Genomic DNA

Fragments

Cloned into a vector

Each fragment sequenced using DNA sequencing method

Re-construction of genome

ATGCCGTAATCGGATCAGTC

Page 6: Presentation on genome sequencing

RECONSTRUCTION OF GENOMES

Clone contig method Shotgun method

Isolation and sequencing of one overlapped clone from library.

Hybridization with second clone

Identification of second clone.

Hybridization of second clone with 3rd clone of library

Randomly generated DNA fragments

Cloning into vector

Sequencing of each clone

Check for overlapping

Assembling of overlapped sequences

Chromosome walking

Page 7: Presentation on genome sequencing
Page 8: Presentation on genome sequencing

The shotgun approach: the genome is randomly broken into short fragments. The resulting sequences are examined for overlaps and these are used to build up the contiguous genome sequence.Used for smaller genome.first used successfully with the bacterium Haemophilus influenzaeThe clone contig approach: involves a pre-sequencing phase a series of overlapping clones is identified. This contiguous series is called a contig.Each piece of cloned DNA is then sequenced, and this sequence placed at its appropriate position on the contig map in order to gradually build up the overlapping genome sequence.

Page 9: Presentation on genome sequencing

2 TYPES OF RECOMBINENT DNA LIBRARIES

GENOMIC/CHROMOSOMAL LIBRARY COMPLEMENTARY DNA (cDNA) LIBRARY

RECOMBINENT DNA LIBRARIES

Page 10: Presentation on genome sequencing

Genomic Library

Complete digestion Mechanical shearing Partial digestion

1. Produces a large number of short DNA clones.

2. Genes containing two or more restriction sites may be cloned in two or more pieces.

1. Produces longer DNA fragments.

2. Ends are not uniform, requires enzymatic modification before fragments can be inserted into a cloning vector.

1. Cut at a less frequent restriction site and limit the amount and time the enzyme is active.

2. Results in population of large overlapping fragments.

3. Selected by agarose electrophoresis.

3 WAYS TO MAKE GENOMIC LIBRARY

Set of recombinant clones that contains all the DNA present in an individual organism

Page 11: Presentation on genome sequencing

Fig. 8.7, Partial digestion with Sau3A

Results in a library of overlapping DNA fragments of various sizes.

Page 12: Presentation on genome sequencing

1. cDNA is derived from mature mRNA, does not include introns.

2. cDNA may contain less information than the coding region.

3. cDNA library reflects gene activity of a cell at the time mRNAs are isolated (varies from tissue to tissue and with time).

4. Creating a cDNA library:

1. Isolate mRNA

2. Synthesize cDNA

3. Clone cDNA

cDNA Library:

Page 13: Presentation on genome sequencing

Fig. 8.15,Synthesis of cDNA

Page 14: Presentation on genome sequencing

Vectors that enable artificial chromosomes to be created and cloned into yeast.

Features:1. Yeast telomere at each end.

2. Yeast centromere sequence.

3. Selectable marker (amino acid dependence, etc.) on each arm.

4. Autonomously replicating sequence (ARS) for replication.

5. Restriction sites (for DNA ligation).

6. Useful for cloning very large DNA fragments up to 500 kb; useful for very large DNA fragments.

Yeast artificial chromosome (YAC)

Page 15: Presentation on genome sequencing

Vectors that enable artificial chromosomes to be created and cloned into E. coli.

Features:

1. Useful for cloning up to 200 kb, but can be handled like regular bacterial plasmid vectors.

2. Useful for sequencing large stretches of chromosomal DNA; frequently used in genome sequencing projects.

3. Like other vectors, BACs contain:

1. Origin (ori) sequence derived from an E. coli plasmid called the F factor.

2. Multiple cloning sites (restriction sites).

3. Selectable markers (antibiotic resistance).

Bacterial artificial chromosome (BAC)